MGRN1
mahogunin ring finger 1
Summary
Enables ubiquitin-protein transferase activity. Involved in endosome to lysosome transport; negative regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway; and protein monoubiquitination. Located in several cellular components, including early endosome; endoplasmic reticulum; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3747587 | 16:4,674,954 | C/A | — | — |
| rs1408772570 | 16:4,674,968 | T/A | — | uncertain significance |
| rs1684609 | 16:4,676,595 | A/G | intron variant | — |
| rs3859158 | 16:4,676,660 | G/A | intron variant | — |
| rs1684608 | 16:4,676,852 | C/A | intron variant | — |
| rs1103156 | 16:4,680,073 | G/A | — | — |
| rs6500625 | 16:4,691,943 | C/T | — | — |
| rs779159728 | 16:4,700,414 | C/T | — | uncertain significance |
| rs35046817 | 16:4,700,418 | C/A | — | benign |
| rs1567190998 | 16:4,700,449 | A/G | — | uncertain significance |
| rs2506216321 | 16:4,700,467 | G/A | — | uncertain significance |
| rs202163970 | 16:4,701,988 | C/A | — | uncertain significance |
| rs755124130 | 16:4,702,004 | C/T | — | uncertain significance |
| rs944959628 | 16:4,702,028 | G/A | — | uncertain significance |
| rs201331866 | 16:4,702,695 | G/A | — | uncertain significance |
| rs376391281 | 16:4,702,758 | G/A | — | uncertain significance |
| rs749894917 | 16:4,702,761 | G/A | — | uncertain significance |
| rs201088254 | 16:4,702,767 | C/T | — | uncertain significance |
| rs780003440 | 16:4,702,768 | G/A | — | uncertain significance |
| rs201958896 | 16:4,702,821 | G/A | — | uncertain significance |
| rs1054921691 | 16:4,707,258 | A/G | — | uncertain significance |
| rs764998848 | 16:4,707,282 | C/G | — | uncertain significance |
| rs758611746 | 16:4,707,284 | G/A | — | uncertain significance |
| rs946956761 | 16:4,707,291 | A/G | — | uncertain significance |
| rs192764498 | 16:4,708,274 | T/A | — | — |
| rs762380681 | 16:4,714,728 | C/G | — | uncertain significance |
| rs369031220 | 16:4,714,734 | G/A | — | uncertain significance |
| rs2078761149 | 16:4,714,773 | G/A | — | uncertain significance |
| rs370162653 | 16:4,715,131 | G/C | — | likely benign |
| rs185620175 | 16:4,716,188 | G/A | intron variant | — |
| rs758776706 | 16:4,718,275 | G/A | — | uncertain significance |
| rs1252165993 | 16:4,723,499 | C/T | — | uncertain significance |
| rs199504452 | 16:4,723,552 | C/T | — | likely benign |
| rs200157628 | 16:4,727,496 | C/T | — | uncertain significance |
| rs767992365 | 16:4,727,538 | G/A | — | uncertain significance |
| rs761140588 | 16:4,730,054 | C/G | — | uncertain significance |
| rs372525104 | 16:4,730,063 | G/A | — | uncertain significance |
| rs967815207 | 16:4,731,566 | C/G | — | uncertain significance |
| rs375493247 | 16:4,731,602 | C/G | — | uncertain significance |
| rs368781016 | 16:4,731,645 | C/T | — | uncertain significance |
| rs200775202 | 16:4,731,672 | G/C | — | uncertain significance |
| rs768292858 | 16:4,731,678 | C/T | — | uncertain significance |
| rs1308339200 | 16:4,731,719 | G/A | — | uncertain significance |
| rs754311885 | 16:4,731,749 | G/T | — | uncertain significance |
| rs779175061 | 16:4,731,750 | G/A | — | uncertain significance |
| rs758808663 | 16:4,731,756 | C/T | — | uncertain significance |
| rs745820631 | 16:4,732,826 | C/A | — | uncertain significance |
| rs371114422 | 16:4,732,832 | G/A | — | uncertain significance |
| rs201280703 | 16:4,732,878 | C/T | — | likely benign |
| rs138756308 | 16:4,732,897 | C/T | — | uncertain significance |
| rs780871722 | 16:4,733,862 | T/C | — | uncertain significance |
| rs1596319306 | 16:4,733,942 | C/G | — | likely benign |
| rs1312339399 | 16:4,733,943 | T/G | — | likely benign |
| rs777933734 | 16:4,738,799 | C/T | — | likely benign |
| rs980567302 | 16:4,738,820 | G/A | — | uncertain significance |
| rs373451060 | 16:4,738,821 | C/A | — | uncertain significance |
| rs533486524 | 16:4,738,832 | G/A | — | uncertain significance |
| rs778024438 | 16:4,738,844 | C/T | — | uncertain significance |
| rs200375426 | 16:4,738,848 | C/T | — | uncertain significance |
| rs1222041314 | 16:4,738,877 | G/C | — | uncertain significance |
| rs139807713 | 16:4,738,891 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.